Research Coordinator - Smidt Heart Institute
Location: Los Angeles
Posted on: November 26, 2022
Grow your career at Cedars-Sinai!The Smidt Heart Institute
reflects Cedars-Sinai's steadfast dedication to heart disease and
research innovation giving patients access to the highest level of
care. Year after year, thousands of people trust their hearts to
Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac
surgeons and niche care teams treat the full spectrum of heart
disease and disorders, while our investigators continue to advance
the field with groundbreaking, life-saving research. From genetic
counseling and targeted drug therapies to a growing array of
minimally invasive procedures, Cedars-Sinai continues to stand at
the forefront of technology, innovation and discovery improving
patient outcomes.Join our team and use your experience with an
organization known nationally for excellence in research!Job
Summary: -The Research Coordinator I prepares and submits protocols
and supporting documents to regulatory bodies such as the IACUC,
and IRB. -This role submits continuations, amendments, responds to
questions, generates reports, and maintains research files and
documentation involving the regulatory requirements for the
study/clinical trial. -Other duties include physical lab
management, ordering and stocking of supplies, representing the
medical center when meeting with pharmaceutical companies,
attending weekly team meetings, and working with other staff to
ensure all regulatory documents and requirements are met and
up-to-date. -Ensures compliance with all federal and local agencies
including the United States Department of Agriculture (USDA) and
the American Association for Laboratory Animal Science
(AALAC).Primary Duties and Responsibilities:
- Submits continuations and amendments as vital to maintain
compliance with regulatory requirements and institutional
- Responds to all questions from the IACUC and/or IRB related to
the regulatory aspects of the study.
- Completes forms and generates all reports vital to align with
regulatory requirements and institutional policies.
- Establishes and maintains research files and documentation
pertaining to regulatory requirements for pre-clinical trials.
- Meets with monitors from pharmaceutical companies and
represents the medical center during these meetings.
- Works closely with the Principal investigator, research staff,
and regulatory staff to assure that all regulatory documents for
the research studies are up-to-date.
- Participates in weekly research team meetings and updates staff
and investigators on the status of regulatory submission and
- May be required to develop budgets.
- Ensures compliance with all federal and local agencies
including the USDA and Internal Animal Care and Use Committee and
the local Institutional Review Board. -
- Participates in required training and education programs.
Educational Requirements:BA/BS degree required, -Masters or MBA
preferredLicenses:N/AExperience:One (1) year directly related
experience, or equivalent combination of education &
experience.Physical Demands:Able to perform moderate lifting. -Able
to sit, stand and walk for prolonged periods of time. -Able to read
papers and online documents. -Able to operate standard office
equipment. -Able to exercise physical ability and perspective
acuity to satisfactorily perform essential job functions. Working
Title:Department:Business Entity:Job Category:Job
Specialty:Position Type:Shift Length:Shift Type:
Keywords: Careerbuilder-US, Los Angeles , Research Coordinator - Smidt Heart Institute, Other , Los Angeles, California
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